Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs11720524 0.882 0.080 3 38633921 intron variant C/G;T snv 0.34 3